Divergent Effects of Oxidatively Induced Modification to the C8 of 2 '-Deoxyadenosine on Transcription Factor Binding: 8,5 '(S)-Cyclo-2 '-deoxyadenosine Inhibits the Binding of Multiple Sequence Specific Transcription Factors, While 8-Oxo-2 '-deoxyadenosine Increases Binding of CREB and NF-kappa B to DNA

作者：Abraham Jessy; Brooks Philip J^*

来源：Environmental and Molecular Mutagenesis, 2011, 52(4): 287-295.

DOI：10.1002/em.20619

• DNA damage
• adenine lesions
• cyclo-dAdo
• 8-oxo-dAdo
• differential binding

DNA is exposed to endogenous and environmental factors that can form stable lesions. If not repaired, these lesions can lead to transcription/replication blocking or mutagenic bypass. Our previous work has focused on 8,5'-cyclopurine 2'-deoxyribonucleosides, a unique class of oxidatively induced DNA lesions that are specifically repaired by the NER pathway (see Brooks PJ [2008]: DNA Repair 7:1168-1179). Here we used EMSA to monitor the ability of sequence-specific transcription factors, HSF1, CREB, and NF-kappaB and "architectural'' transcription factor, HMGA, to bind to their target sequences when 8, 5'(S)-cyclo-2'-deoxyadenosine (cyclo-dAdo) is present within their recognition sequences. For comparison, we also tested the effect of 8-oxo-7,8-dihydro-2'-deoxyadenosine (8-oxo-dAdo) in the same recognition sequences. The presence of a cyclo-dAdo lesion in the target sequence essentially eliminated the binding activity of HSF1, CREB, and NF-kappa B whereas HMGA retained some of its binding activity. In contrast, 8-oxo-dAdo had no obvious effect on the binding activity of HSF1 and HMGA in comparison to lesion-free DNA. Notably, though, CREB and NF kappa B binding increased when an 8-oxo-dAdo lesion was present in their target sequence. Competition EMSA showed about 2-3-fold increased affinity of both proteins for the 8-oxo-dAdo containing target sequence compared to lesion-free DNA. Molecular modeling of the lesions in the NF-kappaB sequence indicated that 8-oxo-dAdo may form an additional hydrogen bond with the protein, thereby strengthening the binding of NF-kappa B to its DNA target. The cyclo-dAdo lesion, in contrast, distorted the DNA structure, providing an explanation for the inhibition of NF-kappaB binding. Environ. Mol. Mutagen. 52:287-295, 2011. Published 2010 Wiley-Liss, Inc.(dagger)

• 出版日期2011-5